U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 2349

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3609657copy number variation667estd214human GRCh37 chr6: 78,892,808-79,053,430 , GRCh38.p12 chr6: 78,183,091-78,343,713 LOC105377865
    esv3605891copy number variation49estd214human GRCh37 chr5: 97,050,505-97,128,253 , GRCh38.p12 chr5: 97,714,801-97,792,549 LOC391813
    esv3605892copy number variation40estd214human GRCh37 chr5: 97,049,822-97,126,058 , GRCh38.p12 chr5: 97,714,118-97,790,354 LOC391813
    esv3609663copy number variation670estd214human GRCh37 chr6: 78,967,097-79,036,275 , GRCh38.p12 chr6: 78,257,380-78,326,558 LOC105377865
    esv3616948copy number variation1095estd214human GRCh37 chr8: 39,231,505-39,288,323 , GRCh38.p12 chr8: 39,373,986-39,430,804 ADAM5
    esv3586506copy number variation1estd214human GRCh37 chr1: 77,243,570-77,295,459 , GRCh38.p12 chr1: 76,777,885-76,829,774 LINC02567
    esv3605890copy number variation54estd214human GRCh37 chr5: 97,047,859-97,096,156 , GRCh38.p12 chr5: 97,712,155-97,760,452 LOC391813
    esv3598497copy number variation28estd214human GRCh37 chr3: 165,039,860-165,084,371 , GRCh38.p12 chr3: 165,322,072-165,366,583 LINC01322
    esv3587491copy number variation2473estd214human GRCh37 chr1: 149,531,789-149,573,452 , GRCh38.p12 chr1: 120,868,540-120,910,198 PPIAL4A
    esv3644983copy number variation2409estd214human GRCh37 chr20: 1,559,739-1,594,685 , GRCh38.p12 chr20: 1,579,093-1,614,039 SIRPB1
    esv3612068copy number variation4estd214human GRCh37 chr7: 7,292,686-7,322,556 , GRCh38.p12 chr7: 7,253,055-7,282,925 LINC03016
    esv3600875copy number variation1672estd214human GRCh37 chr4: 69,425,939-69,455,053 , GRCh38.p12 chr4: 68,560,221-68,589,335 UGT2B17
    esv3620473copy number variation1254estd214human GRCh37 chr9: 43,580,844-43,606,160 , GRCh38.p12 chr9: 42,208,229-42,233,545 LOC112268036
    esv3638686copy number variation852estd214human GRCh37 chr16: 55,798,890-55,822,423 , GRCh38.p12 chr16: 55,764,978-55,788,511 CES1P1
    esv3591709copy number variation1476estd214human GRCh37 chr2: 98,136,216-98,156,567 , GRCh38.p12 chr2: 97,519,753-97,540,104 ANKRD36B
    esv3587880copy number variation879estd214human GRCh37 chr1: 169,224,713-169,245,824 , GRCh38.p12 chr1: 169,255,475-169,276,586 NME7
    esv3628470copy number variation4908estd214human GRCh37 chr12: 8,568,920-8,587,027 , GRCh38.p12 chr12: 8,416,324-8,434,431 OR7E148P
    esv3623140copy number variation1029estd214human GRCh37 chr10: 47,983,067-48,000,904 , GRCh38.p12 chr10: 50,168,602-50,186,441 ASAH2
    esv3615872copy number variation601estd214human GRCh37 chr8: 2,250,517-2,266,603 , GRCh38.p12 chr8|NT_187576.1: 485,727-501,813 LOC105377783
    esv3610079copy number variation3estd214human GRCh37 chr6: 97,193,885-97,211,821 , GRCh38.p12 chr6: 96,746,009-96,763,945 EEF1GP6
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center